首页> 外文期刊>Microbes and infection >Construction of recombinant herpes simplex virus type I expressing green fluorescent protein without loss of any viral genes
【24h】

Construction of recombinant herpes simplex virus type I expressing green fluorescent protein without loss of any viral genes

机译:表达绿色荧光蛋白而不丢失任何病毒基因的重组I型单纯疱疹病毒的构建

获取原文
获取原文并翻译 | 示例
       

摘要

For use in various applications in research on herpes simplex virus type 1, we attempted to generate recombinant HSV-1 expressing green fluorescent protein (GFP) without any loss of viral genes. Our results were as follows. (i) A recombinant HSV-1 (YK333), in which a GFP expression cassette driven by the Egr-1 promoter was inserted into the intergenic region between UL3 and UL4, was constructed. (ii) YK333 replicated as well as wild-type HSV-1 F strain in Vero cells. (iii) As one application of the recombinant YK333 for research on HSV-1, we developed a system to detect anti-herpetic activity, termed a fluorescence-based anti-viral assay. The 50% inhibitory concentration of ganciclovir for YK333 determined using our newly developed assay was comparable to that determined using a plaque reduction assay. YK333 will be a convenient tool for herpes simplex virus research, including such applications as monitoring of viral replication in vitro and in vivo, and rapid screening of potential anti-herpetic agents.
机译:为了在1型单纯疱疹病毒研究中的各种应用中使用,我们尝试生成表达绿色荧光蛋白(GFP)的重组HSV-1,而不会丢失任何病毒基因。我们的结果如下。 (i)构建了重组HSV-1(YK333),其中将由Egr-1启动子驱动的GFP表达盒插入UL3和UL4之间的基因间区域。 (ii)在Vero细胞中复制了YK333以及野生型HSV-1 F株。 (iii)作为重组YK333在HSV-1研究中的一项应用,我们开发了一种检测抗疱疹活性的系统,称为基于荧光的抗病毒测定法。使用我们最新开发的测定法测定的更昔洛韦对YK333的50%抑制浓度与使用噬斑减少测定法测定的浓度相当。 YK333将是用于单纯疱疹病毒研究的便捷工具,包括在体内和体外监测病毒复制以及快速筛选潜在的抗疱疹药物等应用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号